A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17856145



Internal ID22039788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73430943..73430943hg38UCSC Ensembl
chr4:74296660..74296660hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17856145
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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